US6087092A - Compositions and methods for animal husbandry and for treating gastrointestinal disorders - Google Patents
Compositions and methods for animal husbandry and for treating gastrointestinal disorders Download PDFInfo
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- US6087092A US6087092A US09/356,759 US35675999A US6087092A US 6087092 A US6087092 A US 6087092A US 35675999 A US35675999 A US 35675999A US 6087092 A US6087092 A US 6087092A
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- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229940029985 mineral supplement Drugs 0.000 description 1
- 235000020786 mineral supplement Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004118 muscle contraction Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000001020 rhythmical effect Effects 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 235000021391 short chain fatty acids Nutrition 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 235000019195 vitamin supplement Nutrition 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/717—Celluloses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
Definitions
- This invention is in the area of animal feed additives.
- gastrointestinal disorders can be caused by an imbalance in the normal gut flora, usually an increase in harmful bacteria, including pathogenic and putrefactive bacteria such as Clostridium and Bacteroideceae, and/or a decrease in beneficial, acid-forming bacteria such as bifidobacteria.
- Antibiotics have been used to treat diarrhea.
- a major drawback of using antibiotics is that they can be non-selective, killing both the harmful bacteria and the beneficial bacteria.
- Diarrhea is also treated with drugs such as Loperamide HCl, commonly sold under the name ImmodiumTM, and codeine, that act on the smooth muscle in the walls of the gastrointestinal tract to inhibit peristalsis, the rhythmic waves of muscular contraction that move the contents of the GI tubes.
- These drugs are effective to treat the symptoms of diarrhea, which typically include increased force and rate of peristalsis.
- a major limitation, however, is that the cause of the diarrhea is not treated.
- Another approach to treating gastrointestinal disorders involves coating the gastrointestinal tract with a composition containing bismuth salicylate, for example, Pepto-BismolTM.
- a composition containing bismuth salicylate for example, Pepto-BismolTM.
- the limitation with this method of treatment is that bismuth salicylate is not always very effective at treating the symptoms of diarrhea, and does not treat the cause of diarrhea.
- Gastrointestinal disorders have also been treated with dietary fiber. Dietary fiber is a general term covering a number of substances, including cellulose, hemicellulose, oligosaccharides, pectins, gums, waxes, and lignin.
- a more general definition is "endogenous components of plant materials in the diet that are resistant to digestion by human (intestinal) enzymes, i.e., mainly non-starch polysaccharides and lignin.” Grant-Thompson., W., "The Fibre Story,” in Gut Reactions, Understanding Symptoms in the Digestive Tract, Plenum Press, N.Y., pp. 59 (1989). Dietary fiber can be either soluble or insoluble.
- Dietary fiber resists hydrolysis by human alimentary enzymes, but can be fermented by colonic microflora.
- soluble fiber is more readily fermented than insoluble fiber.
- the main physiological effects of these substances are on gastric emptying and colonic transit time, and can result in improved glucose tolerance and decreased starch digestion.
- the fermentation of dietary fiber results in increased bacterial biomass, increased fecal mass, lowering of intracolonic pH due to production of short chain fatty acids, and production of various gases as metabolic end products.
- One limitation of using dietary fiber is that it can decrease the absorption of vitamins in certain individuals.
- dietary fibers are fermented by both harmful and beneficial bacteria.
- lactulose is used clinically to enrich intestinal sugar sources, since lactulose is not digested or absorbed in human intestines, and reaches the ileum intact. While lactulose is digested by bifidobacteria, it is also digested by other intestinal bacteria, such as Escherichia Coli, and sometimes causes diarrhea. Yawaza, K., and Tamura, Z., Bifidobacteria Microflora, 1(1):39-44 (1982). Other examples of dietary fiber that is digested by both beneficial and harmful bacteria are described in Yamada, H., et al., Cereal Foods World, 38(7):490-492, 491 (1993).
- Some dietary fibers are selectively fermented by bifidobacteria, a beneficial bacteria that produces acetic and lactic acid from sugar.
- bifidobacteria a beneficial bacteria that produces acetic and lactic acid from sugar.
- An example of this type of dietary fiber is wheat bran hemicellulose, which is composed mainly of arabinoxylans. Yamada, H., et al., Cereal Foods World, 38(7):490-492 (1993). Wheat bran hemicellulose apparently also suppresses the proliferation of harmful bacteria, such as Escherichia Coli.
- the acid produced by the bifidobacteria suppresses the adsorption of ammonia and amines produced by putrefactive bacteria such as Clostridium.
- Certain compounds can be useful to treat gastrointestinal disorders because they selectively eliminate harmful bacteria.
- Some polyphenols have been reported to be useful for this purpose.
- Certain plants containing polyphenols have been used to treat gastrointestinal disorders. Baldi, A., et al., Planta Medica, 58, Supplemental Issue 1, pp. A691 (1992).
- compositions and methods for treating gastrointestinal disorders in humans and animals It is therefore an object of the present invention to provide compositions and methods for treating gastrointestinal disorders in humans and animals.
- compositions and methods for treating gastrointestinal disorders, including diarrhea, in animals and humans are described.
- the compositions include a dietary fiber in coordination with polyphenol(s). It is believed that the composition acts by increasing the amount of beneficial bacteria, such as bifidobacteria, and reducing the amount of putrefactive and pathogenic bacteria, such as Clostridium.
- the dietary fiber is one or more of cellulose, hemicellulose, oligosaccharides, galactomannan, pectins, gums, waxes, or lignin. Soluble fibers are preferred over insoluble fibers.
- Hemicellulose is a preferred dietary fiber.
- the preferred molecular weight average of the hemicellulose is between 3,000 and 2,500,000, more preferably between 3,000 and 100,000.
- the polyphenols have a preferred molecular weight between 280 and 6,000.
- the ratio by weight of dietary fiber/polyphenols is preferably between 20 and 3.
- Preferred animals to be treated include, but are not limited to humans, pigs, poultry, calves, horses and domestic pets.
- the composition preferably is administered to animals as a food additive, at a dosage level of between 0.1 to 5% by weight of feed, preferably between 0.1 and 2% by weight of feed.
- the composition is administered to humans as a powder added to foodstuff formulations or to drinks.
- a composition and method for treating human gastrointestinal disorders or other disorders in which beneficial moderation of the intestinal microflora or an increase in large intestine pH is sought.
- the composition can also be used to increase the growth rate and to improve feed conversion in animals and to ameliorate or cure scours or diarrhea, and also to improve and maintain general health.
- the composition contains a dietary fiber in combination with polyphenol(s).
- the composition is administered orally to a human or animal in need of treatment of a gastrointestinal disorder, such as diarrhea.
- the composition is believed to lower the concentration of harmful bacteria, for example, putrefactive and pathogenic bacteria, and increase the concentration of beneficial bacteria, such as bifidobacteria.
- harmful bacteria are defined as those bacteria which cause gastrointestinal disorders, and include but are not limited to putrefactive and pathogenic bacteria.
- Putrefactive and pathogenic bacteria are defined as those bacteria that raise colonic pH by producing amines and/or ammonia, p-cresol, and indole. Types of these bacteria include but are not limited to Clostridium spp., Bacteroidaceae, and Candida spp.
- beneficial bacteria are defined as those which increase the amount of small chain fatty acids, such as lactic acid, propionic acid, acetic acid.
- a non-limiting example of a beneficial bacteria is bifidobacteria.
- dietary fiber is defined as endogenous components of plant materials in the diet that are resistant to digestion by human or other animal (intestinal) enzymes.
- Dietary fibers include but are not limited to cellulose, hemicellulose, oligosaccharides, pectins, gums, waxes, and lignin.
- the dietary fiber can be soluble or insoluble, but soluble fibers are preferred.
- Soluble fiber is defined as fiber that is soluble in water, and insoluble fiber is defined as a fiber that is insoluble in water. It is also preferable that the dietary fiber is highly branched, for example, more than one branch per 100 in-chain units.
- Hemicellulose is a preferred dietary fiber.
- hemicellulose is defined as a polysaccharide found in plant cell walls in association with cellulose and lignin, that is soluble in and extractable by dilute alkaline solutions.
- Preferred average molecular weight ranges for hemicelluloses are between 3,000 and 2,500,000, more preferably, between 3,000 and 100,000.
- the hemicellulose is not digested by human alimentary enzymes, reaches the ileum and large intestine largely intact, is not digested by bacteria other than bifidobacteria, and is an efficient sugar source for bifidobacteria.
- the hemicellulose is preferably soluble in aqueous solutions at a pH less than or equal to 8.
- Arabinogalactan is a preferred hemicellulose.
- an arabinogalactan is defined as an oligosaccharide containing a ⁇ -(1,3)-linked galactan backbone with side chains containing arabinose and galactose.
- the average molecular weight is between 3,000 and 2,500,000, and more preferably, between 3,000 and 100,000.
- Preferred arabinogalactans are those derived from Larix trees.
- the ratio of arabino groups to galactose groups is between 0.1:1 and 1:1.
- dietary fibers are known to have bifidogenic factors. These fibers include but are not limited to arabinoxylan, galactomannan, inulin, fructose oligosaccharide, transglycosylated oligosaccharides, and wheat bran hemicellulose. Compositions containing one or more of these fibers in combination with polyphenols are also preferred embodiments.
- polyphenols are defined as molecules with two or more phenol moieties.
- Useful polyphenols include flavonoids, such as tannins, aromadendrines, anthocyanins, catecholins, catechins and taxifolins.
- Taxifolin is a preferred polyphenol since it is found in the Larix tree, which also contains arabinogalactan, a preferred dietary fiber.
- the polyphenol lowers the amount of harmful bacteria, such as Clostridium, without lowering the amount of beneficial bacteria, such as bifidobacteria.
- Preferred polyphenols have a molecular weight range of between 280 and 6,000.
- Dietary fiber and polyphenols are preferably combined by mixing.
- the ratio of fiber/polyphenol by weight in the composition is preferably between 20 and 3.
- This composition can optionally be combined with a carrier that is pharmaceutically acceptable for oral administration.
- the weight percent of the composition/carrier is preferably between 1 and 10.
- Typical carriers are food and water. If soluble fiber is used, the combination of an aqueous carrier and the fiber will be a solution. If insoluble fiber is used, the combination of an aqueous carrier and the fiber will be a suspension.
- compositions can include an inert diluent or an edible carrier. They may be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the composition can be incorporated with excipients and used in the form of tablets, troches, suppositories or capsules. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition.
- the tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
- a binder such as microcrystalline cellulose, gum tragacanth or gelatin
- an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch
- a lubricant such as magnesium stearate or Sterotes
- a glidant such as colloidal silicon dioxide
- dosage unit form When the dosage unit form is a capsule, it can contain, in addition to material of the above type, a liquid carrier such as a fatty oil.
- dosage unit forms can contain various other materials which modify the physical form of the dosage unit, for example, coatings of sugar, shellac, or other enteric agents.
- composition can be administered as a component of an elixir, suspension, syrup, wafer, chewing gum or the like.
- a syrup may contain, in addition to the active compounds, sucrose as a sweetening agent and certain preservatives, dyes and colorings and flavors.
- the composition is useful to treat gastrointestinal disorders, such as diarrhea.
- the composition is administered to a human or animal in need of treatment thereof.
- Gastrointestinal disorders are well known to those in the art. Examples of gastrointestinal disorders include but are not limited to diarrhea, distension of the abdomen, diverticulitis, constipation, and irritable bowel syndrome.
- Several gastrointestinal disorders are known to be caused by an increase in harmful bacteria, or a decrease in beneficial bacteria in the gastrointestinal tract.
- composition is also useful to treat hepatic encephalotomy associated with cirrhosis of the liver.
- Typical systemic dosages for treatment of gastrointestinal disorders are those ranging from 10 mg/kg to 300 mg/kg per day as a single daily dose or divided daily doses.
- composition is administered for a sufficient time period to alleviate the undesired symptoms and the clinical signs associated with the gastrointestinal disorder being treated.
- the concentration of the components in the composition will depend on absorption, inactivation, and excretion rates of the components as well as other factors known to those of skill in the art. It is to be noted that dosage values will also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.
- composition can also be mixed with other active materials which do not impair the desired action, or with materials that supplement the desired action, such as compounds that treat the symptoms of peristalsis.
- the dietary fiber-polyphenol composition can be added to animal feed.
- Animal feeds include but are not limited to poultry feed, swine feed, horse feed, feed for early-weaned calves, and dog and cat food.
- Typical dosage ranges are between 0.1 to 5% by weight of the animal feed, preferably between 0.1 and 2% by weight of the animal feed.
Abstract
Description
Claims (16)
Priority Applications (1)
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US27841494A | 1994-07-21 | 1994-07-21 | |
US09/356,759 US6087092A (en) | 1994-07-21 | 1999-07-19 | Compositions and methods for animal husbandry and for treating gastrointestinal disorders |
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US09/356,759 Expired - Lifetime US6087092A (en) | 1994-07-21 | 1999-07-19 | Compositions and methods for animal husbandry and for treating gastrointestinal disorders |
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US08/434,492 Expired - Lifetime US5614501A (en) | 1994-07-21 | 1995-05-04 | Compositions and methods for animal husbandry and for treating gastrointestinal disorders |
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US (2) | US5614501A (en) |
EP (1) | EP0797451B1 (en) |
AT (1) | ATE277638T1 (en) |
DE (1) | DE69533593T2 (en) |
WO (1) | WO1996003150A1 (en) |
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Also Published As
Publication number | Publication date |
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DE69533593D1 (en) | 2004-11-04 |
DE69533593T2 (en) | 2005-10-13 |
ATE277638T1 (en) | 2004-10-15 |
EP0797451B1 (en) | 2004-09-29 |
US5614501A (en) | 1997-03-25 |
WO1996003150A1 (en) | 1996-02-08 |
EP0797451A2 (en) | 1997-10-01 |
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